# Nexgen Medical Systems, Inc.

- Location (FDA's records): Melbourne, FL
- FDA decisions: 4 (2009–2011): 4 510(k) clearances
- Product codes: QEZ (1), DYB (1), QEW (1), DQY (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Baxter Healthcare Corp: 1 (https://510kreport.com/company/baxter-healthcare)
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)
- Applied Medical: 1 (https://510kreport.com/company/applied-medical)
- Cordis Corp.: 1 (https://510kreport.com/company/cordis)
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)

## Firms that cite its devices most
- Surmodics,Inc.: 1 (https://510kreport.com/company/surmodics)

## Its most-cited devices
- K110315: Nexgen Peripheral Mechanical Retrieval Device (2011), cited by 1
- K090932: Nexgen Peripheral Mechanical Retrieval Device - 200CM, Model MRD-1000; 80  CM, Model MRD-2000 (2009), cited by 1

## Recent decisions
- K102925: Nexgen Expandable Catheter (Nov 10, 2011)
- K110315: Nexgen Peripheral Mechanical Retrieval Device (Oct 20, 2011)
- K102979: Nexgen Peripheral Guide Catheter (Jan 18, 2011)
- K090932: Nexgen Peripheral Mechanical Retrieval Device - 200CM, Model MRD-1000; 80  CM, Model MRD-2000 (Sep 24, 2009)

Source page: https://510kreport.com/company/nexgen-medical-systems